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10
immersion thermometer, digital thermocouple thermometer, not a total immersion thermometer) placed in
1
the designated location, verify that the 3M Molecular Detection Heat Block Insert is at 100 ±1°C.
2
G. P
REPARATION OF THE
3MM
OLECULAR
D
ETECTION
I
NSTRUMENT
3
1.
Launch the 3M™ Molecular Detection Software and log in.
4
2.
Turn on the 3M Molecular Detection Instrument.
5
3.
Create or edit a run with data for each sample. Refer to the 3M Molecular Detection
6
System User Manual for details.
7
8
NOTE:
The 3M Molecular Detection Instrument must reach and maintain temperature of 60°C before
9
inserting the 3M Molecular Detection Speed Loader Tray with reaction tubes. This heating step takes
10
approximately 20 minutes and is indicated by an ORANGE light on the instrument’s status bar. When the
11
instrument is ready to start a run, the status bar will turn GREEN.
12
H. L
YSIS
13
1.
Allow the lysis solution (LS) tubes to warm up by setting the rack at room temperature (20-
14
25 °C) overnight (16-18 hours). Alternatives to equilibrate the LS tubes to room
15
temperature are to set the LS tubes on the laboratory bench for at least 2 hours, incubate the
16
LS tubes in a 37 ±1°C incubator for 1 hour or place them in a dry double block heater for
17
30 seconds at 100°C.
18
2.
Invert the capped tubes to mix. Proceed to next step within 4 hrs.
19
3.
Remove the enrichment broth from the incubator.
20
4.
One LS tube is required for each sample and the Negative Control (NC) (sterile enrichment
21
medium) sample.
22
4.1
LS tube strips can be cut to desired LS tube number. Select the number of individual LS
23
tubes or 8-tube strips needed. Place the LS tubes in an empty rack.
24
4.2
To avoid cross-contamination, decap one LS tubes strip at a time and use a new pipette
25
tip for each transfer step.
26
4.3
Transfer enriched sample to LS tubes as described below:
27
28
Transfer each enriched sample into individual LS tube
first
. Transfer the NC
last
.
29
30
4.4
Use the 3M™ Molecular Detection Cap/Decap Tool-Lysis to decap one LS tube strip -
31
one strip at a time.
32
4.5
Discard the LS tube cap – if lysate will be retained for retest, place the caps into a clean
33
container for re-application after lysis
34
4.6
Transfer 20 µL of sample into a LS tube.
35
5.
Repeat step 4.2 until each individual sample has been added to a corresponding LS tube in
36
the strip as illustrated below.
37
38
39
AOAC Research Institute
Expert R view Panel Use Only
OMAMAN-29 A/ Collaboartive Study Manuscript
OMA ERP June 2016
ERP Use Only